Cargando…

Gastrointestinal, vaginal, nasopharyngeal, and breast milk microbiota profiles and breast milk metabolomic changes in Gambian infants over the first two months of lactation: A prospective cohort study

Microbiota composition in breast milk affects intestinal and respiratory microbiota colonization and the mucosal immune system’s development in infants. The metabolomic content of breast milk is thought to interact with the microbiota and may influence developing infant immunity. One hundred seven G...

Descripción completa

Detalles Bibliográficos
Autores principales: Karampatsas, Konstantinos, Faal, Amadou, Jaiteh, Mustapha, Garcia-Perez, Isabel, Aller, Sean, Shaw, Alexander G., Kopytek, Aleksandra, Witney, Adam A., Le Doare, Kirsty
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9678627/
https://www.ncbi.nlm.nih.gov/pubmed/36401392
http://dx.doi.org/10.1097/MD.0000000000031419
_version_ 1784834029747437568
author Karampatsas, Konstantinos
Faal, Amadou
Jaiteh, Mustapha
Garcia-Perez, Isabel
Aller, Sean
Shaw, Alexander G.
Kopytek, Aleksandra
Witney, Adam A.
Le Doare, Kirsty
author_facet Karampatsas, Konstantinos
Faal, Amadou
Jaiteh, Mustapha
Garcia-Perez, Isabel
Aller, Sean
Shaw, Alexander G.
Kopytek, Aleksandra
Witney, Adam A.
Le Doare, Kirsty
author_sort Karampatsas, Konstantinos
collection PubMed
description Microbiota composition in breast milk affects intestinal and respiratory microbiota colonization and the mucosal immune system’s development in infants. The metabolomic content of breast milk is thought to interact with the microbiota and may influence developing infant immunity. One hundred seven Gambian mothers and their healthy, vaginally delivered, exclusively breastfed infants were included in our study. We analyzed 32 breast milk samples, 51 maternal rectovaginal swabs and 30 infants’ rectal swabs at birth. We also analyzed 9 breast milk samples and 18 infants’ nasopharyngeal swabs 60 days post-delivery. We used 16S rRNA gene sequencing to determine the microbiota composition. Metabolomic profiling analysis was performed on colostrum and mature breast milk samples using a multiplatform approach combining 1-H Nuclear Magnetic Resonance Spectroscopy and Gas Chromatography-Mass Spectrometry. Bacterial communities were distinct in composition and diversity across different sample types. Breast milk composition changed over the first 60 days of lactation. α-1,4- and α-1,3-fucosylated human milk oligosaccharides, and other 33 key metabolites in breast milk (monosaccharides, sugar alcohols and fatty acids) increased between birth and day 60 of life. This study’s results indicate that infant gut and respiratory microbiota are unique bacterial communities, distinct from maternal gut and breast milk, respectively. Breast milk microbiota composition and metabolomic profile change throughout lactation. These changes may contribute to the infant’s immunological, metabolic, and neurological development and could consist the basis for future interventions to correct disrupted early life microbial colonization.
format Online
Article
Text
id pubmed-9678627
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Lippincott Williams & Wilkins
record_format MEDLINE/PubMed
spelling pubmed-96786272022-11-22 Gastrointestinal, vaginal, nasopharyngeal, and breast milk microbiota profiles and breast milk metabolomic changes in Gambian infants over the first two months of lactation: A prospective cohort study Karampatsas, Konstantinos Faal, Amadou Jaiteh, Mustapha Garcia-Perez, Isabel Aller, Sean Shaw, Alexander G. Kopytek, Aleksandra Witney, Adam A. Le Doare, Kirsty Medicine (Baltimore) 6200 Microbiota composition in breast milk affects intestinal and respiratory microbiota colonization and the mucosal immune system’s development in infants. The metabolomic content of breast milk is thought to interact with the microbiota and may influence developing infant immunity. One hundred seven Gambian mothers and their healthy, vaginally delivered, exclusively breastfed infants were included in our study. We analyzed 32 breast milk samples, 51 maternal rectovaginal swabs and 30 infants’ rectal swabs at birth. We also analyzed 9 breast milk samples and 18 infants’ nasopharyngeal swabs 60 days post-delivery. We used 16S rRNA gene sequencing to determine the microbiota composition. Metabolomic profiling analysis was performed on colostrum and mature breast milk samples using a multiplatform approach combining 1-H Nuclear Magnetic Resonance Spectroscopy and Gas Chromatography-Mass Spectrometry. Bacterial communities were distinct in composition and diversity across different sample types. Breast milk composition changed over the first 60 days of lactation. α-1,4- and α-1,3-fucosylated human milk oligosaccharides, and other 33 key metabolites in breast milk (monosaccharides, sugar alcohols and fatty acids) increased between birth and day 60 of life. This study’s results indicate that infant gut and respiratory microbiota are unique bacterial communities, distinct from maternal gut and breast milk, respectively. Breast milk microbiota composition and metabolomic profile change throughout lactation. These changes may contribute to the infant’s immunological, metabolic, and neurological development and could consist the basis for future interventions to correct disrupted early life microbial colonization. Lippincott Williams & Wilkins 2022-11-18 /pmc/articles/PMC9678627/ /pubmed/36401392 http://dx.doi.org/10.1097/MD.0000000000031419 Text en Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle 6200
Karampatsas, Konstantinos
Faal, Amadou
Jaiteh, Mustapha
Garcia-Perez, Isabel
Aller, Sean
Shaw, Alexander G.
Kopytek, Aleksandra
Witney, Adam A.
Le Doare, Kirsty
Gastrointestinal, vaginal, nasopharyngeal, and breast milk microbiota profiles and breast milk metabolomic changes in Gambian infants over the first two months of lactation: A prospective cohort study
title Gastrointestinal, vaginal, nasopharyngeal, and breast milk microbiota profiles and breast milk metabolomic changes in Gambian infants over the first two months of lactation: A prospective cohort study
title_full Gastrointestinal, vaginal, nasopharyngeal, and breast milk microbiota profiles and breast milk metabolomic changes in Gambian infants over the first two months of lactation: A prospective cohort study
title_fullStr Gastrointestinal, vaginal, nasopharyngeal, and breast milk microbiota profiles and breast milk metabolomic changes in Gambian infants over the first two months of lactation: A prospective cohort study
title_full_unstemmed Gastrointestinal, vaginal, nasopharyngeal, and breast milk microbiota profiles and breast milk metabolomic changes in Gambian infants over the first two months of lactation: A prospective cohort study
title_short Gastrointestinal, vaginal, nasopharyngeal, and breast milk microbiota profiles and breast milk metabolomic changes in Gambian infants over the first two months of lactation: A prospective cohort study
title_sort gastrointestinal, vaginal, nasopharyngeal, and breast milk microbiota profiles and breast milk metabolomic changes in gambian infants over the first two months of lactation: a prospective cohort study
topic 6200
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9678627/
https://www.ncbi.nlm.nih.gov/pubmed/36401392
http://dx.doi.org/10.1097/MD.0000000000031419
work_keys_str_mv AT karampatsaskonstantinos gastrointestinalvaginalnasopharyngealandbreastmilkmicrobiotaprofilesandbreastmilkmetabolomicchangesingambianinfantsoverthefirsttwomonthsoflactationaprospectivecohortstudy
AT faalamadou gastrointestinalvaginalnasopharyngealandbreastmilkmicrobiotaprofilesandbreastmilkmetabolomicchangesingambianinfantsoverthefirsttwomonthsoflactationaprospectivecohortstudy
AT jaitehmustapha gastrointestinalvaginalnasopharyngealandbreastmilkmicrobiotaprofilesandbreastmilkmetabolomicchangesingambianinfantsoverthefirsttwomonthsoflactationaprospectivecohortstudy
AT garciaperezisabel gastrointestinalvaginalnasopharyngealandbreastmilkmicrobiotaprofilesandbreastmilkmetabolomicchangesingambianinfantsoverthefirsttwomonthsoflactationaprospectivecohortstudy
AT allersean gastrointestinalvaginalnasopharyngealandbreastmilkmicrobiotaprofilesandbreastmilkmetabolomicchangesingambianinfantsoverthefirsttwomonthsoflactationaprospectivecohortstudy
AT shawalexanderg gastrointestinalvaginalnasopharyngealandbreastmilkmicrobiotaprofilesandbreastmilkmetabolomicchangesingambianinfantsoverthefirsttwomonthsoflactationaprospectivecohortstudy
AT kopytekaleksandra gastrointestinalvaginalnasopharyngealandbreastmilkmicrobiotaprofilesandbreastmilkmetabolomicchangesingambianinfantsoverthefirsttwomonthsoflactationaprospectivecohortstudy
AT witneyadama gastrointestinalvaginalnasopharyngealandbreastmilkmicrobiotaprofilesandbreastmilkmetabolomicchangesingambianinfantsoverthefirsttwomonthsoflactationaprospectivecohortstudy
AT ledoarekirsty gastrointestinalvaginalnasopharyngealandbreastmilkmicrobiotaprofilesandbreastmilkmetabolomicchangesingambianinfantsoverthefirsttwomonthsoflactationaprospectivecohortstudy